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通过多重聚合酶链反应(PCR)检测和rpoB序列测定鉴定弧菌分离株。

Identification of Vibrio isolates by a multiplex PCR assay and rpoB sequence determination.

作者信息

Tarr Cheryl L, Patel Jayna S, Puhr Nancy D, Sowers Evangeline G, Bopp Cheryl A, Strockbine Nancy A

机构信息

Foodborne and Diarrheal Diseases Branch, Division of Bacterial and Mycotic Diseases, National Center for Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, GA 30333, USA.

出版信息

J Clin Microbiol. 2007 Jan;45(1):134-40. doi: 10.1128/JCM.01544-06. Epub 2006 Nov 8.

Abstract

Vibrio, a diverse genus of aquatic bacteria, currently includes 72 species, 12 of which occur in human clinical samples. Of these 12, three species--Vibrio cholerae, Vibrio parahaemolyticus, and Vibrio vulnificus-account for the majority of Vibrio infections in humans. Rapid and accurate identification of Vibrio species has been problematic because phenotypic characteristics are variable within species and biochemical identification requires 2 or more days to complete. To facilitate the identification of human-pathogenic species, we developed a multiplex PCR that uses species-specific primers to amplify gene regions in four species (V. cholerae, V. parahaemolyticus, V. vulnificus, and V. mimicus). The assay was tested on a sample of 309 Vibrio isolates representing 26 named species (including 12 human pathogens) that had been characterized by biochemical methods. A total of 190 isolates that had been identified as one of the four target species all yielded results consistent with the previous classification. The assay identified an additional four V. parahaemolyticus isolates among the other 119 isolates. Sequence analysis based on rpoB was used to validate the multiplex results for these four isolates, and all clustered with other V. parahaemolyticus sequences. The rpoB sequences for 12 of 15 previously unidentified isolates clustered with other Vibrio species in a phylogenetic analysis, and three isolates appeared to represent unnamed Vibrio species. The PCR assay provides a simple, rapid, and reliable tool for identification of the major Vibrio pathogens in clinical samples, and rpoB sequencing provides an additional identification tool for other species in the genus Vibrio.

摘要

弧菌属是一类多样的水生细菌,目前包括72个种,其中12种出现在人类临床样本中。在这12种中,有三种——霍乱弧菌、副溶血性弧菌和创伤弧菌——占人类弧菌感染的大多数。由于种内表型特征多变且生化鉴定需要2天或更长时间才能完成,弧菌种的快速准确鉴定一直存在问题。为便于鉴定人类致病菌种,我们开发了一种多重聚合酶链反应(PCR),该方法使用种特异性引物扩增四种弧菌(霍乱弧菌、副溶血性弧菌、创伤弧菌和模仿弧菌)的基因区域。该检测方法在309株弧菌分离株的样本上进行了测试,这些分离株代表26个已命名的种(包括12种人类病原体),此前已通过生化方法进行了鉴定。总共190株被鉴定为四种目标菌种之一的分离株所产生的结果均与先前的分类一致。该检测方法在其他119株分离株中又鉴定出4株副溶血性弧菌分离株。基于rpoB的序列分析用于验证这4株分离株的多重PCR结果,所有结果均与其他副溶血性弧菌序列聚类。在系统发育分析中,15株先前未鉴定的分离株中有12株的rpoB序列与其他弧菌种聚类,3株分离株似乎代表未命名的弧菌种。该PCR检测方法为临床样本中主要弧菌病原体的鉴定提供了一种简单、快速且可靠的工具,而rpoB测序为弧菌属中的其他菌种提供了额外的鉴定工具。

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